Naya-Català Fernando, Piazzon M Carla, Torrecillas Silvia, Toxqui-Rodríguez Socorro, Calduch-Giner Josep À, Fontanillas Ramón, Sitjà-Bobadilla Ariadna, Montero Daniel, Pérez-Sánchez Jaume
Nutrigenomics and Fish Growth Endocrinology Group, Institute of Aquaculture Torre de la Sal (IATS, CSIC), 12595 Castellón, Spain.
Fish Pathology Group, Institute of Aquaculture Torre de la Sal (IATS, CSIC), 12595 Castellón, Spain.
Biology (Basel). 2022 Nov 30;11(12):1744. doi: 10.3390/biology11121744.
Fish genetically selected for growth (GS) and reference (REF) fish were fed with CTRL (15% FM, 5-7% FO) or FUTURE (7.5% FM, 10% poultry meal, 2.2% poultry oil + 2.5% DHA-algae oil) diets during a 12-months production cycle. Samples from initial (t; November 2019), intermediate (t; July 2020) and final (t; November 2020) sampling points were used for Illumina 16S rRNA gene amplicon sequencing of the adherent microbiota of anterior intestine (AI). Samples from the same individuals (t) were also used for the gene expression profiling of AI by RNA-seq, and subsequent correlation analyses with microbiota abundances. Discriminant analyses indicated the gut bacterial succession along the production cycle with the proliferation of some valuable taxa for facing seasonality and different developmental stages. An effect of genetic background was evidenced along time, decreasing through the progression of the trial, namely the gut microbiota of GS fish was less influenced by changes in diet composition. At the same time, these fish showed wider transcriptomic landmarks in the AI to cope with these changes. Our results highlighted an enhanced intestinal sphingolipid and phospholipid metabolism, epithelial turnover and intestinal motility in GS fish, which would favour their improved performance despite the lack of association with changes in gut microbiota composition. Furthermore, in GS fish, correlation analyses supported the involvement of different taxa with the down-regulated expression of pro-inflammatory markers and the boosting of markers of extracellular remodelling and response to bacterium. Altogether, these findings support the combined action of the gut microbiome and host transcriptionally mediated effects to preserve and improve gut health and function in a scenario of different growth performance and potentiality.
在为期12个月的生产周期中,对经过生长基因选育的鱼类(GS)和对照鱼类(REF)投喂CTRL日粮(15%鱼粉,5 - 7%鱼油)或FUTURE日粮(7.5%鱼粉,10%禽肉粉,2.2%禽油 + 2.5%DHA藻油)。分别在初始(t;2019年11月)、中期(t;2020年7月)和末期(t;2020年11月)采样点采集样本,用于对前肠(AI)附着微生物群进行Illumina 16S rRNA基因扩增子测序。来自相同个体(t)的样本也用于通过RNA测序对AI进行基因表达谱分析,以及随后与微生物群丰度的相关性分析。判别分析表明,随着生产周期的推进,肠道细菌发生演替,一些应对季节性和不同发育阶段的有价值分类群出现增殖。随着时间的推移,遗传背景的影响逐渐显现,在试验过程中这种影响逐渐减弱,即GS鱼类的肠道微生物群受饮食组成变化的影响较小。与此同时,这些鱼类在前肠表现出更广泛的转录组特征以应对这些变化。我们的结果突出显示,GS鱼类的肠道鞘脂和磷脂代谢、上皮更新以及肠道运动增强,这将有助于其性能提升,尽管这与肠道微生物群组成的变化缺乏关联。此外,在GS鱼类中,相关性分析支持不同分类群参与促炎标志物表达下调以及细胞外重塑和对细菌反应标志物的增强。总之,这些发现支持肠道微生物群和宿主转录介导效应的联合作用,以在不同生长性能和潜力的情况下维持和改善肠道健康与功能。